Tag | Content |
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EnhancerAtlas ID | HS145-01435 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr1:117079840-117080580 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
DMRT3 | MA0610.1 | chr1:117080478-117080489 | ATTGATACATT | - | 6.62 | JUN(var.2) | MA0489.1 | chr1:117080338-117080352 | ATGAGTCATTTATT | - | 6.38 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_09788 | chr1:117079120-117088914 | CD14 | SE_19688 | chr1:117079352-117081415 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_28774 | chr1:117080386-117082718 | Fetal_Intestine_Large | SE_32513 | chr1:117080479-117089910 | GM12878 | SE_59077 | chr1:117079459-117152311 | Ly3 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 117080047 | 117080432 | chr1 | 117080073 | 117080476 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I116537 | chr1 | 117078903 | 117082377 |
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Enhancer Sequence | CACACAGTGG GCTATGATTG CATCAGACTG AGACCTTGTC TTTAAATATA TAGGAATGAA 60 GTAAATACTT GTTCCTATGC TTGACCCATA GGGTGCTCCC CATAATTAAG TGGGGTGCTT 120 AATATGCAGA GGAAATACTT TGTATTACCT TTCCAAAATG TAAAAAAAAA TTTTAATTCC 180 ATAACACGTC TGACTCAAAG CATTTTGTGA AAGGAAAGTC CATAATACAT CTGACTCAAT 240 ACATTTTGTG AAAGGTGGAG CTACACAGAG CCTTGTCGGG CCCTGCCTAT TGGTTGGGCT 300 GGACCTGTTA ATAGGCAGTG CAGGGAGCAG CATGTGTCAC AGACCTGCCT GTCCAGAGGC 360 CTCACTCCCA CCCTTCTTCT AGGAAGTGCC TCCTATTGGC TAAGGCAGCA TGGACCTACA 420 AGGATGAGTT AAGACACTAA CATGTCACAT TCTGCCATTG TTGCCCTTTA AAAGCCTCAA 480 GGCTAATTAC TTTGTCCTAT GAGTCATTTA TTTGTTAATT CATATGCCTT CTTGCGTCTC 540 AGCTACCCTC CAGCAATTAA TCATAAGAGG CCTGAGGAAA CATGCAAAAA CATATGTAAT 600 ATACAACAAT GGTCATGGTA GCACTGGGAT AATAAAGTAT TGATACATTA TAAACGTCTA 660 CTAAAAAGAG CATTTAAGTA AATTTAGGTT CACCAAGATA ATGGAATACT ATGTTGTCAT 720 TTAAAATGAT GTTTTCTAAG 740
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